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Completed Phase 3 Interventional Results available

Study to Evaluate the Efficacy and Safety of APL-2 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

ClinicalTrials.gov ID: NCT03500549

Public ClinicalTrials.gov record NCT03500549. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 4:41 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III, Randomized, Multi-Center, Open-Label, Active-Comparator Controlled Study to Evaluate the Efficacy and Safety of APL-2 in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)

Study identification

NCT ID
NCT03500549
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Apellis Pharmaceuticals, Inc.
Industry
Enrollment
80 participants

Conditions and interventions

Interventions

  • Pegcetacoplan Drug
  • Soliris Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 13, 2018
Primary completion
Nov 13, 2019
Completion
Aug 12, 2020
Last update posted
Mar 24, 2022

2018 – 2020

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
University of Southern California Los Angeles California 90033
Sarcoma Oncology Research Center Santa Monica California 90403
Denver Health Denver Colorado 80204
Georgetown University Hospital Washington D.C. District of Columbia 20057
Cancer Specialists of North Florida Jacksonville Florida 32256
Lakes Research Miami Lakes Florida 33014
Mid Florida Hematology and Oncology Orange City Florida 32763
Winship Cancer Institute of Emory University Atlanta Georgia 30322
Northwestern University Chicago Illinois 60611
Investigative Clinical Research of Indiana Indianapolis Indiana 46260
Cancer & Hematology Centers of Western Michigan Grand Rapids Michigan 49503
Roswell Park Cancer Institute Buffalo New York 14263
New York Cancer & Blood Specialists East Setauket New York 11733
New York Cancer & Blood Specialists The Bronx New York 10469
Duke University Medical Center Durham North Carolina 27710
Good Samaritan Hospital Corvallis Oregon 97330
University of Tennessee Medical Center Knoxville Tennessee 37920
Baptist Cancer Center Memphis Tennessee 38120
HOPE Cancer Center of East Texas Tyler Texas 75701

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 34 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03500549, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 24, 2022 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03500549 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →